Classifications

• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
  • D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
  • D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
  • D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
  • D01F9/127—Carbon filaments; Apparatus specially adapted for the manufacture thereof by thermal decomposition of hydrocarbon gases or vapours or other carbon-containing compounds in the form of gas or vapour, e.g. carbon monoxide, alcohols
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B82—NANOTECHNOLOGY
  • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
  • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
  • D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
  • D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
  • D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
  • D01F9/127—Carbon filaments; Apparatus specially adapted for the manufacture thereof by thermal decomposition of hydrocarbon gases or vapours or other carbon-containing compounds in the form of gas or vapour, e.g. carbon monoxide, alcohols
  • D01F9/133—Apparatus therefor
• • H—ELECTRICITY
  • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
  • H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
  • H05K1/00—Printed circuits
  • H05K1/02—Details
  • H05K1/03—Use of materials for the substrate
  • H05K1/0313—Organic insulating material
  • H05K1/0353—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement
  • H05K1/0373—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement containing additives, e.g. fillers
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S977/00—Nanotechnology
  • Y10S977/70—Nanostructure
  • Y10S977/734—Fullerenes, i.e. graphene-based structures, such as nanohorns, nanococoons, nanoscrolls or fullerene-like structures, e.g. WS2 or MoS2 chalcogenide nanotubes, planar C3N4, etc.
  • Y10S977/742—Carbon nanotubes, CNTs
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S977/00—Nanotechnology
  • Y10S977/70—Nanostructure
  • Y10S977/773—Nanoparticle, i.e. structure having three dimensions of 100 nm or less
  • Y10S977/775—Nanosized powder or flake, e.g. nanosized catalyst
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S977/00—Nanotechnology
  • Y10S977/70—Nanostructure
  • Y10S977/832—Nanostructure having specified property, e.g. lattice-constant, thermal expansion coefficient
  • Y10S977/835—Chemical or nuclear reactivity/stability of composition or compound forming nanomaterial
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S977/00—Nanotechnology
  • Y10S977/70—Nanostructure
  • Y10S977/832—Nanostructure having specified property, e.g. lattice-constant, thermal expansion coefficient
  • Y10S977/835—Chemical or nuclear reactivity/stability of composition or compound forming nanomaterial
  • Y10S977/836—Chemical or nuclear reactivity/stability of composition or compound forming nanomaterial having biological reactive capability
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S977/00—Nanotechnology
  • Y10S977/84—Manufacture, treatment, or detection of nanostructure
  • Y10S977/842—Manufacture, treatment, or detection of nanostructure for carbon nanotubes or fullerenes
  • Y10S977/843—Gas phase catalytic growth, i.e. chemical vapor deposition

Definitions

• the present invention relates to a method for forming carbon nanofibers, which are also known as nanotubes, by means of a generated plasma and chemically assisted catalysis.
• Carbon fibers hold great promise as a high-performance material for use in composites due to their high strength and high modulus. They are commonly made by elevating a precursor material such as polyacrylonitrile (PAN) or pitch in an inert atmosphere to a temperature around 1000°C on continuous wind-up devices.
• PAN polyacrylonitrile
• the fibers formed by this process are generally continuous filaments and approximately 8 ⁇ m in diameter.
• Carbon nanofibers have been produced directly from hydrocarbons in a gas phase reaction upon contact with a catalytic metal particle when heated by thermal energy to around 1000°C in a non-oxidizing gas stream.
• Carbon nanofibers differ physically from commercial carbon fibers in that they are thinner and are not continuous. Typically, they have a length around 0.01 mm to 0.1 mm and have a diameter generally of 10nm to 100nm.
• Carbon nanofibers also differ functionally from commercial carbon fibers in that they have a higher thermal conductivity, have high electrical conductivity, and are less subject to etching. Accordingly, carbon nanofibers offer great promise in a number of applications.
• Carbon nanotubes are structures which consist of a sheet of carbon atoms in graphene forms wrapped into a cylinder.
• a single walled nanotube has only a single atomic layer.
• Multiwalled nanotubes have additional layers of carbon deposited pyrolytically. Multiwalled nanotubes may thus contain 100 to 1000 atomic layers.
• Multiwalled nanotubes have excellent strength, small diameter (typically less than 200 nm) and near-metallic electrical conductivity, making them useful as an additive to enhance structural properties of composites such as carbon-carbon, carbon-epoxy, carbon-metal, carbon-plastic, carbon-polymer and carbon-concrete.
• Carbon nanotubes have been produced by arc-evaporation chemical reactions and by pyrolysis reactions using lasers to initiate pyrolysis. However, these methods are not effective for producing significant quantities of nanofibers. Thus, a need exists in the art for a method which can reliably and effectively produce carbon nanofibers in significant quantities.
• the present invention provides a method for making carbon nanofibers and nanotubes which is quick and efficient. By being quick and efficient, it has the potential to be less expensive than currently used methods.
• carbon nanofibers are formed in a reactor.
• the process includes the steps of: providing, in a reactor, a first catalyst in the form of solid catalytic particles; applying a vacuum to the reactor to create a reduced pressure in the reactor; feeding a first mixture of gases including a carbon-based gas into the reactor; forming, from the carbon-based gas, a plasma containing carbon free-radical species; and forming, in the presence of the catalytic particles, the carbon free-radical species into carbon nanofibers.
• the first mixture of gases also includes hydrogen gas which is provided to inhibit pyrolytic fattening of the carbon nanofibers and to inhibit the formation of soot during the reaction. It is also desirable that the process includes the additional step of feeding a growth catalyst gas into the reactor to cause the fibers to increase diametrically in size.
• the carbon nanofibers of the present invention can be further processed to form a carbon-carbon matrix material.
• the process includes the following additional steps: increasing the concentration of the carbon-based gas in the first mixture of gases to form a second mixture of gases; pyrolyzing the second mixture of gases to deposit a bulk layer of carbon on the carbon nanofibers forming a carbon-carbon matrix material which contains carbon nanofibers throughout its thickness; and removing the matrix material from the reactor.
• a gaseous catalyst can be used to facilitate formation of the carbon nanofibers.
• This aspect of the process includes the following steps: applying a vacuum to the reactor to create a reduced pressure in the reactor; feeding a mixture of gases including a carbon- based gas into the reactor; feeding a catalyst gas into the reactor; forming, from the carbon-based gas, a plasma containing carbon free-radical species; and forming, in the presence of the catalyst gas, the carbon free-radical species into carbon nanofibers.
• the mixture of gases also includes hydrogen gas which is provided to inhibit pyrolytic fattening of the carbon nanofibers as they are being formed and to inhibit the formation of soot during the reaction. It is also desirable with the process that the process also includes the additional step of feeding a growth catalyst gas into the reactor to cause the fibers to increase diametrically in size.
• the carbon nanofibers of the present invention can be further processed to form a carbon-carbon matrix material.
• the process includes the following additional steps: increasing the concentration of the carbon-based gas in the first mixture of gases to form a second mixture of gases; pyrolyzing the second mixture of gases to deposit a bulk layer of carbon on the carbon nanofibers forming a carbon-carbon matrix material which contains carbon nanofibers throughout its thickness; and removing the matrix material from the reactor.
• the present invention is also directed to a process for forming a carbon- epoxy matrix material.
• This process comprises the following steps: providing, in a reactor, solid catalyst particles on a substrate; feeding a mixture of gases including a hydrogen gas and a carbon-based gas into the reactor; forming, from the carbon-based gas, a plasma containing carbon free-radical species; forming, in the presence of the catalytic particles, the carbon free-radical species into carbon nanofibers; removing the substrate bearing the carbon nanofibers from the reactor; forming a mold in which a portion of the mold is formed by the substrate; infiltrating the mold with an epoxy composition to form a carbon-epoxy matrix material containing carbon nanofibers throughout its thickness; and removing the matrix material from the mold.
• Fig. 1 is a photomicrograph of the carbon nanostructures formed by the process of this invention.
• Fig. 2 is a photomicrograph showing the crosslinking of the carbon nanostructures formed by the process of this invention.
• Fig. 3 is a schematic representation of the equipment used to produce carbon nanostructures via microwave dissociation.
• the method of this invention produces carbon nanostructures such as those shown in Figs. 1 and 2.
• Fig. 1 is a photomicrograph at 750X magnification and
• Fig. 2 is a photomicrograph at 15,000X magnification.
• the fibers, shown in Figs. 1 and 2 have a diameter of about 100 nm, which is about three orders of magnitude smaller than conventional pitch or PAN-based fibers. For that reason, these fibers are referred to as being "nanofibers.”
• the fibers typically have a length of about 1-2 mm. Thus, they have an aspect ration (L/d) of about 1x10 4 and a surface area to volume ratio of about 1x10 14 n ⁇ 1 .
• L/d aspect ration
• the individual fibers tend to cross-link with each other which increases the capacity of the fibers to conduct heat and electricity.
• These fibers also have a high level of graphitization which further increases their high thermal conductivity and provides near-metallic electrical conductivity.
• the carbon nanofibers are formed by a chemical catalysis of a plasma formed from a carbon-based gas.
• the plasma is formed by means of the plasma generator.
• the plasma generating source is a microwave generator, a hot -5-
• a mixture of gases including the carbon-based gas, are provided in a reactor.
• these gases which form the mixture, are fed into the reactor from tanks containing the respective gases.
• the formation of the fibers is carried out at a reduced pressure of from about 10 Torr to about 100 Torr and, desirably, from about 20 Torr to about 50 Torr.
• the carbon-based gas is formed into a plasma in the presence of a first catalyst in the reactor.
• the mixture of gases can be formed into a plasma by means of a plasma generating source such as a microwave generator, a hot filament, an RF generator or an electrical discharge.
• the first catalyst can be either in the form of solid catalytic particles or in a gaseous state.
• the substrate has a temperature from about 800°C to about 1200°C and, desirably, a temperature from 800°C to about 1000°C.
• the mixture of gases also includes hydrogen gas.
• the hydrogen gas is provided to inhibit pyrolytic fattening of the nanofibers and to inhibit the formation of soot during the pyrolysis reaction.
• carbon nanofibers are formed by the chemically catalyzed deposition of carbon from the carbon free-radical species generated in the plasma.
• a second catalyst in the form of a growth catalyst gas may also be used to promote diametric growth of the fibers.
• carbon atoms are dissociated from the carbon-based gas and a plasma is formed which contains carbon and hydrocarbon free-radicals. Then the carbon is captured by the catalyst to form the carbon nanofibers. The entire process requires no more than about one hour of time from start to finish.
• the carbon-based gas must be a gas which forms carbon and hydrocarbon free-radical species upon pyrolysis.
• the carbon-based gas used to form the carbon fibers is at least one gas selected from the group consisting of carbon dioxide, methane, ethane, propane, ethene, natural gas and coal derivative gases.
• the carbon-based gas may also be a mixture of these gases. More desirably, the carbon-based gas is methane.
• the gas mixture used to form the carbon fibers includes from about 40% to about 90% of hydrogen gas and from about 10% to about 60% of the carbon-based gas. More desirably, the gas mixture comprises about a 50-50 mixture of hydrogen gas and the carbon-based gas.
• the gas flow for the fiber formation reaction measures from about 20 seem to about 1000 seem and desirably is about 100 seem.
• the first catalyst is provided in the form of solid particles having a size from about 10 nm to about 1 micron.
• the first catalyst is selected from the group consisting of iron containing materials, nickel containing materials, cobalt containing materials and sulfur containing materials.
• Useful materials for the first catalyst include, but are not limited to, iron, nickel, cobalt, ferrocene, iron pentacarbonyl, alloys of iron, alloys of nickel, alloys of cobalt, sulfur, hydrogen sulfide, iron sulfide, and nickel nitrate.
• the first catalyst is iron sulfide. It is believed that the particles of the first catalyst serve to nucleate the fibers and cause the beginning of fiber formation. Typically, from about 10 mg to about 100 mg of the first catalyst in the form of particles is used to form 10 mg of fibers.
• a second, growth catalyst gas may also be used in combination with the hydrogen gas and the carbon-based gas to modify the surface properties of the fibers.
• the growth catalyst is applied to "fatten" the fibers, i.e., it is a second catalyst which promotes diametric growth of the fiber.
• Useful growth catalysts include hydrogen, ammonia and mixtures thereof. Desirably, the growth catalyst will be ammonia.
• the first catalyst can be provided in a gaseous state rather than being provided as solid particles. If the first catalyst is used in a gaseous state, it may be supplied in combination with the hydrogen gas and the carbon-based gas simultaneously as a mixture of gases. In this reaction, the carbon nanofibers are produced on a steady state basis and are collected as they form. If the first catalyst is in the gaseous form, it will be selected from the group consisting of iron pentacarbonyl, hydrogen sulfide, and a ferrocene-xylene mixture.
• a deposition apparatus 10 useful for forming the carbon nanofibers shown in Figs. 1 and 2 is shown in Fig. 3.
• the apparatus 10 comprises a plasma reactor 12, a series of gas tanks 14, and a vacuum pump 16. Gas tanks 14 feed gas into reactor 12 and pump 16 is provided to create a reduced pressure in reactor 12.
• Reactor 12 is desirably a microwave reactor such as an ASTEX microwave reactor available from Applied Science and Technology of Woburn, Massachusetts, U.S.A.
• Pump 16 can be a conventional mechanical vacuum pump.
• a useful vacuum pump is available from Varian Vacuum Products of Lexington, Massachusetts, U.S.A.
• Pump 16 desirably includes an associated pressure measuring device, which is desirably a baratron device.
• Reactor 12 includes a power supply 20, a feed tube 22 and a waveguide 24.
• Power supply 20 provides reactor 12 with a source of energy.
• reactor 12 is a microwave reactor and power supply 20 is a microwave generator.
• the energy source used to form the plasma from the carbon-based gas is desirably microwave energy.
• Feed tube 22 is disposed in reactor 12 and extends generally axially therein. Desirably, feed tube 22 extends along more than 1 of the length of reactor 12 and more desirably extends along more than % of the length of reactor 12.
• Waveguide 24 extends from power supply 20 to feed tube 22. Waveguide 24 directs energy from power supply 20 to feed tube 22.
• Reactor 12 and feed tube 22 are desirably constructed of a material which is resistant to heat and corrosion. Suitable materials include nickel, high temperature steel, quartz, ceramic, and refractory materials. Desirably, feed tube 22 is formed from quartz. An optional catch basin 46 may be positioned at one end of feed tube 22. Catch basin 46 is used to collect fibers formed when the first catalyst is a gas.
• Gas tanks 14 include a hydrogen gas tank 30, a carbon-based gas tank 32, an optional tank 34 for containing the growth catalyst, and an optional tank 36 for containing a gaseous catalyst. Gas tanks 30, 32, 34 and 36 are connected to feed -8-
• the apparatus 10 may also include an optical pyrometer 42.
• Pyrometer 42 is used instead of a thermocouple because thermocouples are susceptible to interaction with the field of plasma generated in reactor 12.
• a substrate (not shown) is used to support the first catalyst in reactor 12.
• the substrate is desirably formed from an inert dielectric material such as quartz, ceramic and refractory materials. Desirably, the substrate is ceramic. Metals, such as molybdenum, titanium and nickel may also be used.
• the first catalyst in the form of solid catalytic particles, is placed on the substrate which is then positioned in feed tube 22.
• the substrate and first catalyst particles are positioned so that they are positioned in about the center of feed tube 22 at the intersection of waveguide 24 and feed tube 22.
• the substrate can be positioned in feed tube 22 on a rod which is desirably an aluminum oxide rod.
• the pressure in feed tube 22 is reduced by means of vacuum pump 16. A total vacuum is not created in feed tube 22 but the pressure is reduced to a pressure measuring from about 10 Torr to about 100 Torr and, desirably, from about 20 Torr to about 50 Torr.
• the gases from the hydrogen gas tank 30 and carbon-based gas tank 32 are fed through the gas lines 38 and combined to form a mixture of gases which is fed from tanks 14 through gas lines 36 to feed tube 22.
• mass flow controllers 40 control the flow of gases from tanks 14 to feed tube 22.
• the gas flow will be provided at a rate from about 20 seem to about 1000 seem and desirably at about 100 seem.
• the energy is conveyed from power supply 20 to feed tube 22 through waveguide 24.
• power supply 20 requires from about 600 Watts to about 1200 Watts of power.
• the flow of energy from power supply 20 is discontinued, the gas flow is ceased and the fibers are removed from the reactor 12.
• the growth catalyst gas is supplied from tank 34 simultaneously with the hydrogen gas and the carbon-based gas in the mixture of gases.
• the first catalyst can be provided to feed tube 22 in a gaseous state rather than being provided as solid particles. If the first catalyst is used in a gaseous state, it will be provided from tank 36 through gas lines 38 to feed tube 22. It may be supplied to feed tube 22 in combination with the hydrogen gas and the carbon-based gas simultaneously as a mixture of gases.
• the first catalyst is formed into a plasma in feed tube 22 by means of the energy generated by the power supply 20 along with the hydrogen gas and the carbon-based gas. In this embodiment of the process of this invention, no substrate or solid catalyst particles are needed. Instead, the carbon nanofibers are produced on a steady state basis and, for that reason, it is necessary to supply apparatus 10 at one end of feed tube 22 with a catch basin, such as catch basin 46, in which the fibers can be collected.
• the carbon nanofibers formed by the above described processes of this invention have several applications.
• the high level of graphitization and crosslinking allows these fibers to efficiently conduct heat. By being able to efficiently conduct heat, these fibers can be used to provide thermal management systems such as heat sinks for use in computers and printed circuit boards.
• the high aspect ratio allows these fibers to be used to shield electro-magnetic interference and to absorb radio frequency and microwave energy.
• the fibers formed by the method of this invention can be used to form high thermal conductivity cold plates for standard electronic module (SEM) boards and other electronic cooling applications such as heat sinks for high -10-
• SEM standard electronic module
• the fibers may also be used as an additive to provide improved strength and reinforcement to plastics, rubber, concrete, epoxies, and other materials.
• the carbon fibers can also be used as a replacement for carbon in rubber applications. At higher concentrations, the fibers could be used to form an electrically conductive rubber. Because of their high electrical conductivity and small volume, the fibers can be used as an obscurant for microwaves, radio frequencies and other electromagnetic interferences.
• the fibers can also be used to form passive heat sinks for high heat flux devices. Electrically and thermally conductive adhesives and fillers can be formulated with the carbon nanofibers as the key component. Finally, they can be used to absorb oil slicks on bodies of water because of their high surface area.
• the carbon nanofibers formed by the process of this invention can be further processed to form a matrix material, such as a carbon-carbon matrix material or a carbon-epoxy matrix material, having an increased strength modulus, electrical conductivity and thermal conductivity.
• a matrix material such as a carbon-carbon matrix material or a carbon-epoxy matrix material, having an increased strength modulus, electrical conductivity and thermal conductivity.
• the carbon nanofibers can be formed by either of the above described methods.
• the fibers are not removed from reactor 12. Instead, the flow of gases into feed tube 22 is adjusted to form a second mixture of gases.
• This second mixture of gases is formulated to contain a higher concentration of the carbon-based gas.
• the second mixture of gases will contain from about 0% to about 60% of the hydrogen gas and from about 40% to about 100% of the carbon-based gas.
• a different gas such as one of those listed above, may be used as the carbon-based gas in forming the carbon matrix.
• the reaction is not delayed by changes to the gas supply.
• the increased concentration of carbon-based gas in the second mixture of gases forms a bulk carbon layer which infiltrates the carbon nanofibers to form a carbon-carbon matrix material.
• the matrix material is then removed from reactor 12 and can then be processed further for its desired use.
• a matrix material may also be formed through the use of epoxy -11-
• the substrate is removed from the reactor without removing the fibers from the substrate.
• the substrate is then used to form a portion of a mold used to make the matrix material. The remainder of the mold is formed so that it incorporates the substrate.
• An epoxy material is then poured into the mold and so that it infiltrates the mass of fibers in the mold.
• the epoxy material is then cured so that the epoxy material and the carbon nanofibers form a matrix material.
• the matrix material is removed from the mold and the substrate.
• the resulting matrix material comprises a carbon-epoxy matrix material which has high conductivity carbon nanofibers throughout its thickness.
• the carbon- epoxy matrix material can also be compression molded to a desired shape before being removed from the mold.

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• Engineering & Computer Science (AREA)
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• Textile Engineering (AREA)
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• Condensed Matter Physics & Semiconductors (AREA)
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